Search details
1.
Cis- and trans-eQTL TWASs of breast and ovarian cancer identify more than 100 susceptibility genes in the BCAC and OCAC consortia.
Am J Hum Genet
; 2024 May 02.
Article
in English
| MEDLINE | ID: mdl-38723630
2.
Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons.
Am J Hum Genet
; 109(8): 1500-1519, 2022 08 04.
Article
in English
| MEDLINE | ID: mdl-35931052
3.
Identification of PSMB5 as a genetic modifier of fragile X-associated tremor/ataxia syndrome.
Proc Natl Acad Sci U S A
; 119(22): e2118124119, 2022 05 31.
Article
in English
| MEDLINE | ID: mdl-35617426
4.
POIROT: a powerful test for parent-of-origin effects in unrelated samples leveraging multiple phenotypes.
Bioinformatics
; 39(4)2023 04 03.
Article
in English
| MEDLINE | ID: mdl-37067493
5.
Familial aggregation of seizure outcomes in four familial epilepsy cohorts.
Epilepsia
; 2024 May 13.
Article
in English
| MEDLINE | ID: mdl-38738647
6.
Novel Variance-Component TWAS method for studying complex human diseases with applications to Alzheimer's dementia.
PLoS Genet
; 17(4): e1009482, 2021 04.
Article
in English
| MEDLINE | ID: mdl-33798195
7.
Association of inflammation-related exposures and ovarian cancer survival in a multi-site cohort study of Black women.
Br J Cancer
; 129(7): 1119-1125, 2023 10.
Article
in English
| MEDLINE | ID: mdl-37537254
8.
Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes.
Hum Genet
; 142(10): 1531-1541, 2023 Oct.
Article
in English
| MEDLINE | ID: mdl-37676273
9.
Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios.
Am J Hum Genet
; 107(1): 124-136, 2020 07 02.
Article
in English
| MEDLINE | ID: mdl-32574564
10.
Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting.
Genet Med
; 25(10): 100918, 2023 10.
Article
in English
| MEDLINE | ID: mdl-37330696
11.
Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?
Am J Med Genet A
; 191(10): 2558-2570, 2023 10.
Article
in English
| MEDLINE | ID: mdl-37350193
12.
FAT4 identified as a potential modifier of orofacial cleft laterality.
Genet Epidemiol
; 45(7): 721-735, 2021 10.
Article
in English
| MEDLINE | ID: mdl-34130359
13.
TIGAR: An Improved Bayesian Tool for Transcriptomic Data Imputation Enhances Gene Mapping of Complex Traits.
Am J Hum Genet
; 105(2): 258-266, 2019 08 01.
Article
in English
| MEDLINE | ID: mdl-31230719
14.
Behavioral changes and growth deficits in a CRISPR engineered mouse model of the schizophrenia-associated 3q29 deletion.
Mol Psychiatry
; 26(3): 772-783, 2021 03.
Article
in English
| MEDLINE | ID: mdl-30976085
15.
Efficient estimation of indirect effects in case-control studies using a unified likelihood framework.
Stat Med
; 41(15): 2879-2893, 2022 07 10.
Article
in English
| MEDLINE | ID: mdl-35352841
16.
Rare variants in MYH15 modify amyotrophic lateral sclerosis risk.
Hum Mol Genet
; 28(14): 2309-2318, 2019 07 15.
Article
in English
| MEDLINE | ID: mdl-30985904
17.
The "maternal effect" on epilepsy risk: Analysis of familial epilepsies and reassessment of prior evidence.
Ann Neurol
; 87(1): 132-138, 2020 01.
Article
in English
| MEDLINE | ID: mdl-31637767
18.
Epilepsy in families: Age at onset is a familial trait, independent of syndrome.
Ann Neurol
; 86(1): 91-98, 2019 07.
Article
in English
| MEDLINE | ID: mdl-31050039
19.
Generalized, focal, and combined epilepsies in families: New evidence for distinct genetic factors.
Epilepsia
; 61(12): 2667-2674, 2020 12.
Article
in English
| MEDLINE | ID: mdl-33098311
20.
PEMapper and PECaller provide a simplified approach to whole-genome sequencing.
Proc Natl Acad Sci U S A
; 114(10): E1923-E1932, 2017 03 07.
Article
in English
| MEDLINE | ID: mdl-28223510